Clinical Study Coordinator (LPN or RN) - Ophthalmology, Gynecology & Special Studies
Clinical Research Laboratories, LLC - Piscataway, NJ 08854
Nurse Clinical Coordinator/CRC/ Clinical Research
Clinical Study Coordinator – Ophthalmology, Gynecology & Special Studies/Clinical Services (Full-Time) Do you have an LPN or RN degree in Nursing? Do you want to work in a well-established clinical lab assessing the safety and efficacy of personal care products? If so, this position may be for you.
Compensation commensurate with experience. Highly qualified candidates are preferred and will be actively considered.
About the Company:
Clinical Research Laboratories, LLC (CRL) is an independent clinical research laboratory that provides a wide range of clinical safety and efficacy tests to the cosmetic, beauty products, personal care, and pharmaceutical industries. The lab is located in Piscataway Township, near Rutgers University in central New Jersey. Approximately 100 people work for the company.
About the Position:
This is a full time, salaried position, conducting clinical research studies. The position requires the candidate to have a basic knowledge of Good Clinical Practices and to act as Principal Investigator for studies as assigned, conducting dermal, ophthalmic and/or gynecologic examinations according to protocol requirements.
About the Interview Process:
A proficiency test may be given for detail orientation. Hours: Monday through Friday, 8:00 AM to 5:00 PM.
LPN or RN in Nursing
Ophthalmic experience a plus
Exceptional detail orientation.
Excellent verbal and written communication skills.
Ability to be a self-starter and work cooperatively with other professionals in a medium-sized company environment.
Good typing skills.
Proficiency in Office Software programs.
Desired Qualifications: LPN or RN
Previous experience conducting clinical research studies
Experience following SOPs. Experience interacting with scientists or working in a scientific field. Experience in a GCP-compliant lab.
Excellent interpersonal skills
Interact with Investigators, Sponsors, Statisticians and any other resources necessary to assist, as needed, in critical protocol design.
Assure that study protocol meets all requirements of sponsor.
Designate an individual to serve as a project manager and assume the primary responsibility for the conduct of a study.
Provide responsible individuals with the signed protocol, panelist requirements, study requirements and scheduling information.
Assure all required equipment, supplies and consultants are available for the conduct of the study and that visits are scheduled appropriately.
Prepare documentation necessary for IRB submission.
Provide Sponsor and company management with progress reports as required.
Supervise the conduct of studies and assist in the conduct of the study as required.
Perform dermal, Ophthalmic and/or Gynecological examinations or other evaluations on subjects, as required by protocol.
Review and interpret study results as needed.
Provide daily work direction, training and guidance to all directly reporting staff.
Respond to Sponsor request for information, study timelines and interim results.
Compensation and Benefits:
Compensation commensurate with experience.
Highly qualified candidates are preferred and will be actively considered.
2 weeks paid vacation after one year of service.
Health insurance benefits and retirement savings plan.
Respond to this posting. Attach your resume and make the subject line of the email the word "Clinical Study Coordinator" then your name and a one-word description of your best professional attribute. Please do not call the laboratory. Someone from the lab will contact you if more information or an interview is desired.
· Principals only. Recruiters please do not contact this job poster.
· Do NOT contact us with unsolicited services or offers
· Do NOT contact us if you are not cleared to work in the United States
· Do Not contact us if your do not have a nursing license from the United States
Salary-Commensurate with experience
Career Level Required-Experience necessary
Experience Required-Clinical Research Experience
Education Required-LPN or RN license
Job Status-Full Time
Job Type: Full-time